EP1754497A1 - Méthode et système pour déterminer une quantité efficace d'énergie à délivrer à un fluide lors d'une photothérapie - Google Patents

Méthode et système pour déterminer une quantité efficace d'énergie à délivrer à un fluide lors d'une photothérapie Download PDF

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EP1754497A1
EP1754497A1 EP06075929A EP06075929A EP1754497A1 EP 1754497 A1 EP1754497 A1 EP 1754497A1 EP 06075929 A EP06075929 A EP 06075929A EP 06075929 A EP06075929 A EP 06075929A EP 1754497 A1 EP1754497 A1 EP 1754497A1
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light energy
fluid
targets
value
target
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EP1754497B1 (fr
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Kyu Ho Lee
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Therakos Inc
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Therakos Inc
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3681—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits by irradiation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3681—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits by irradiation
    • A61M1/3683—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits by irradiation using photoactive agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3687—Chemical treatment
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3693—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging
    • A61M1/3696—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3693—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/05—General characteristics of the apparatus combined with other kinds of therapy
    • A61M2205/051—General characteristics of the apparatus combined with other kinds of therapy with radiation therapy
    • A61M2205/053—General characteristics of the apparatus combined with other kinds of therapy with radiation therapy ultraviolet

Definitions

  • This invention generally relates to determining an amount of light energy to deliver to fluids, particularly partially transparent fluids, containing targets for the light energy, in order to deliver an effective amount of light energy to the targets.
  • the invention particularly relates to phototherapy and photopheresis systems where an effective amount of light energy is desired to be delivered to targets in biological fluids.
  • UV light irradiation or phototherapy has been widely used in the chemical and biological sciences for many years.
  • Ultraviolet (UV) light irradiation of blood was used in the 1930's, 40's, and 50's for the treatment of many conditions.
  • These conditions included bacterial diseases such as septicemias, pneumonias, peritonitis, wound infection, viral infections including acute and chronic hepatitis, poliomyelitis, measles, mumps, and mononucleosis.
  • Phototherapy or light irradiation also includes the processes of exposing photoactivatable or photosensitizable targets, such as cells, blood products, bodily fluids, chemical molecules, tissues, viruses, and drug compounds, to light energy, which induces an alteration in or to the targets.
  • photoactivatable or photosensitizable targets such as cells, blood products, bodily fluids, chemical molecules, tissues, viruses, and drug compounds.
  • applications of phototherapy are increasing in the medical field. These applications include the inactivation of viruses contaminating blood or blood products, the preventive treatment of platelet-concentrate infusion-induced alloimmunization reactions, and the treatment of both autoimmune and T-cell mediated diseases.
  • Light irradiation applications also include the irradiation sterilization of fluids that contain undesirable microorganisms, such as bacteria or viruses.
  • Light irradiation may be effective to eliminate immunogenicity in cells, inactivate or kill selected cells, inactivate viruses or bacteria, or activate desirable immune responses.
  • phototherapy can be used as an antiviral treatment for certain blood components or whole blood.
  • a pathogenic virus in a donated platelet concentrate can be inactivated by UV light exposure.
  • photoactivatable drugs may involve treating the blood of a diseased patient where specific blood cells have become pathogenic as a consequence of the disease state.
  • the methods generally may involve treating the pathogenic blood cells, such as lymphocytes, with a photoactivatable drug, such as a psoralen, which is capable of forming photoadducts with lymphocyte DNA when exposed to UV radiation.
  • ECP extracorporeal photopheresis
  • An application of ECP is for the treatment of cutaneous T-cell lymphoma (CTCL).
  • CCL cutaneous T-cell lymphoma
  • 8-MOP 8-methoxypsoralen
  • blood is withdrawn from the patient, anticoagulated, and the white cells are separated by centrifugation and collected as a leukocyte enriched fraction, also known as the buffy coat.
  • the 8-MOP molecules in the blood enter the white blood cell nuclei and intercalate in its double-stranded DNA helix.
  • UV light is directed at the leukocyte-enriched blood fraction and promotes the photoactivation of the target 8-MOP molecules.
  • the photoactivated 8-MOPs alter the pathogenic leukocyte by cross-linking to the thymidine bases and prevent the unwinding of DNA during transcription.
  • the fluid containing the altered leukocytes is then reinfused back into the patient.
  • the reinfusion induces a therapeutically significant delayed immune attack that targets antigens on the surface of both irradiated and unirradiated leukocytes of the same pathogenic clones. See PCT Application WO 97/36581 entitled Photopheresis Treatment of Leukocytes, which is expressly hereby incorporated herein by reference in its entirety.
  • ECP also has been shown to be an effective therapy in a number of autoimmune diseases such as progressive systemic sclerosis (see A.H. Rook et al., ARCH. DERMATOL. 128:337-346 (1992) ), inflammatory bowel disease, rheumatoid arthritis (see S. Malawista, et al., ARTHRITIS RHEUM. 34:646-654 (1991) ), and juvenile onset diabetes mellitus (see J. Ludvigsson, DIABETES METAB. REV.
  • autoimmune diseases such as progressive systemic sclerosis (see A.H. Rook et al., ARCH. DERMATOL. 128:337-346 (1992) ), inflammatory bowel disease, rheumatoid arthritis (see S. Malawista, et al., ARTHRITIS RHEUM. 34:646-654 (1991) ), and juvenile onset diabetes mellitus (see J. Ludvigsson,
  • the ECP treatment preferably results in a highly specific immune response against aberrant T-cells as well as removal of pathogenic antibodies and circulating immune complexes.
  • Stacking occurs in a fluid when material or targets in the fluid are not distributed uniformly on the fluid surface but rather are located at different depths throughout the fluid. Therefore, for instance, targets in the outer most layer of the fluid, closest to the irradiating light source, may be exposed to incident light intensity, while the targets below the surface layer may receive attenuated light energy.
  • non-targets in the biological fluid may include red blood cells, which have discoid shapes with depressions at the middle.
  • red blood cells When red blood cells are aligned parallel to the light energy source during irradiation, their attenuation of light is minimized.
  • red blood cells are aligned perpendicular to the light energy source during irradiation, their attenuation of light is maximized.
  • the CTCL ECP methodology referenced in PCT Application WO 97/36581 can be used to illustrate these exemplary light attenuation characteristics.
  • the buffy coat suspension usually contains some red blood cells and platelets due to inefficiencies inherent in the cell separation techniques utilized. Since the buffy coat suspension, red blood cells and platelets are not completely transparent, they can attenuate the light energy during irradiation. Also, since the fluid's thickness during irradiation can support target white blood cells at different depths, stacking is present. Finally, the alignment of red blood cells in the fluid containing the buffy coat may attenuate the light energy.
  • the desired amount of light energy for delivery to targets may be result-based, e.g., delivering enough light energy to the target white blood cells to produce a gradual death rate culminating in at least fifty (50) percent of treated, irradiated white blood cells dead after day six (6) of irradiation.
  • the fluid's non-transparent qualities presently make it difficult to accurately calculate the amount of light energy required to deliver to the fluid, in order to achieve the desired result.
  • a conventional way to reduce the effect of the attenuation of light in such applications is to constantly agitate the fluid during irradiation. Agitation assists to produce uniform exposure of the targets to the light energy, yet it does not directly address all the light attenuating factors present in such applications. See PCT Application WO 98/22164 , entitled Blood Product Irradiation Device Incorporating Agitation, which is expressly incorporated herein by reference.
  • the present invention relates to methods and systems for determining the effective amount of light energy for delivery to a fluid containing targets, and delivering said light energy to the targets.
  • the fluid is a biological fluid.
  • the fluid light energy value FLEV
  • TELEV target's effective light energy value
  • ALE Factor average light energy factor of the fluid
  • a computer processor may be used to determine the FLEV.
  • the fluid containing the targets is a biological fluid. More preferably, the biological fluid comprises leukocyte-rich buffy coat. The leukocyte-rich buffy coat may be treated with a light energy activatable drug. More preferably, the buffy coat may be treated with 8-MOP. In another embodiment of the present invention, the fluid is a homogenous biological fluid.
  • the biological fluid may also comprise non-target materials. These non-target materials may attenuate the light energy, and affect calculation of the FLEV. Non-target materials may consist of red blood cells.
  • the light energy delivered to the targets may be UV light energy. More preferably, the light energy is ultraviolet A (UVA) light energy.
  • UVA ultraviolet A
  • the effective light energy value of the targets may be obtained by accessing an effective light energy value table.
  • the effective light energy value of the targets may be obtained by placing the targets in fluid and irradiating the fluid with sample light energy values.
  • the selected fluid may limit the attenuation of the delivered light energy.
  • the fluid may consist of saline. More specifically, leukocyte-rich buffy coat targets may be placed in saline and irradiated to identify a light energy value whereby a desired percentage of the leukocytes will gradually die over the course of a specified time after exposure to the light energy.
  • the selected fluid may consist of plasma. Sample biological fluids may be obtained from donors. The targets in the sample fluids may then be irradiated with sample light energy values to identify the effective light energy value.
  • a computer processor may be used to determine the effective light energy value of the targets.
  • the fluid's average light energy factor may be determined by accessing a light energy factor table.
  • a computer processor may be used to determine the average light energy factor.
  • the average light energy factor may be calculated from the measurements of an average light energy value at a unit surface area of the targets in the biological fluid and a light energy value at an incident surface of the biological fluid film.
  • the average light energy at unit surface area of the targets in the biological fluid may be obtained by accessing an average light energy at unit surface area table.
  • the light energy value at an incident surface may also be obtained by accessing a light energy value at an incident surface table.
  • the average light energy factor may be calculated from the measurements of a thickness ratio and a light transmittance value of a known fluid thickness.
  • the thickness ratio may be obtained by accessing a thickness ratio table.
  • the irradiation period may be obtained by accessing a light transmittance value of a known fluid thickness.
  • the thickness ratio may be calculated from the uniform thickness for said biological fluid and the thickness for said non-targets. Further, the uniform thickness for the biological fluid may be obtained by accessing a uniform thickness table, while the thickness for non-targets may be obtained by accessing a non-target thickness table.
  • the average light energy factor may be calculated from the measurements of a thickness ratio and the red blood cell percentage of the biological fluid.
  • the red blood cell percentage may be obtained by accessing a red blood cell percentage table.
  • Another method for calculating the average light energy factor may utilize the measurements of the uniform thickness of the biological fluid and the red blood cell percentage of the biological fluid.
  • the equations used in this method may preferably be used for red blood cell concentrations in the biological fluid of up to about twenty (20) percent, and more preferably for red blood cell concentrations of up to about seven (7) to eight (8) percent.
  • theoretical stacking of red blood cells may not occur. In another embodiment, stacking of red blood cells may occur and a factor may be obtained. This factor may, in a particular embodiment, be between 1 and 2, and more particularly about 1.5.
  • the irradiation time period required by a light energy source to deliver the FLEV may be calculated once the target's effective light energy value and the fluid's average light energy factor have been determined using one of the methods of the present invention and used to calculate the FLEV.
  • the irradiation time period may be calculated from measurements of a volume of biological fluid value, a percent of red blood cells value and a decay life value.
  • a computer system may be used to determine the FLEV.
  • This computer system may comprise a processor, memory and a computer process. More specifically, the computer process may comprise an obtainer configured to obtain the effective light energy value of the target, an obtainer configured to obtain the average light energy factor of the fluid and/or a calculator configured to calculate the FLEV.
  • the calculator used to calculate the FLEV may also be configured to calculate an irradiation time period over which the FLEV is delivered to the targets.
  • the calculator used to calculate the FLEV may also contain an obtainer to obtain a decay life value for the light energy source.
  • the calculator may also contain an obtainer to obtain a volume of biological fluid value and an obtainer to obtain a percent of red blood cells value.
  • the obtainer configured to obtain the effective light energy value of the targets may include an accessor configured to access a light energy factor table.
  • the obtainer configured to obtain the effective light energy value of the targets may include an obtainer configured to obtain the average light energy value at a unit surface area of the targets, an obtainer configured to obtain a light energy value at an incident surface of the biological fluid and/or a calculator configured to calculate the average light energy factor.
  • the obtainer configured to obtain a light energy value at an incident surface of the biological fluid may contain an accessor configured to access an average light energy value at an incident surface of the biological fluid table, and/or an accessor configured to access an average light energy value at unit surface area table.
  • the obtainer configured to obtain an average light energy factor may contain an obtainer configured to obtain a thickness ratio, an obtainer configured to obtain a light transmittance value of a known fluid thickness and/or a calculator configured to calculate the average light energy factor for the biological fluid. More preferably, the obtainer configured to obtain a thickness ratio may contain an accessor configured to access a thickness ratio table, and the obtainer configured to obtain a light transmittance value of a known fluid thickness may contain an accessor configured to access a light transmittance value of a known fluid thickness table.
  • the obtainer configured to obtain the thickness ratio may include an obtainer configured to obtain a uniform thickness for the biological fluid, an obtainer configured to obtain a thickness for the non-targets and/or a calculator configured to calculate the thickness ratio. More preferably, the obtainer configured to obtain a uniform thickness for the biological fluid may contain an accessor configured to access a uniform thickness table, and the obtainer configured to obtain a thickness for the non-targets may contain an accessor configured to access a non-target thickness table.
  • the obtainer configured to obtain the average light energy factor may include an obtainer configured to obtain a red blood cell percentage for the biological fluid. More preferably, the obtainer configured to obtain a red blood cell percentage may contain an accessor configured to access a red blood cell percentage table.
  • the obtainer configured to obtain the thickness ratio may include an obtainer configured to obtain a uniform thickness for the biological fluid, an obtainer configured to obtain a thickness for the non-targets and a calculator configured to calculate the thickness ratio. More preferably, the obtainer configured to obtain the uniform thickness may contain an accessor configured to access a uniform thickness table, and the obtainer configured to obtain the thickness of the non-targets may contain an accessor configured to access a non-target thickness table.
  • the obtainer configured to obtain the average light energy factor may include an obtainer configured to obtain a red blood cell percentage for the biological fluid.
  • the computer system may further include an obtainer configured to obtain the red blood cell stacking factor.
  • the stacking factor may be between 1 and 2. More particularly, the stacking factor may be 1.5.
  • the present invention also relates to a computer readable medium containing instructions for controlling a computer system used to perform the methods described herein for determining a fluid light energy value for delivery to a biological fluid comprising targets, wherein an effective amount of light energy is delivered to the targets.
  • Methods and articles of manufacture consistent with the present invention may involve the functions and operations performed by the described systems and the components thereof.
  • Light irradiation methodologies involve the delivery of light energy to a target to achieve a desired result.
  • the targets may be carried in a medium (e.g., a fluid) during light irradiation.
  • a medium e.g., a fluid
  • the amount of light energy delivered to targets in a fluid that contains essentially no non-target light attenuating material, in order to achieve the desired result is the TELEV.
  • non-target materials may also be present in the fluid, which may result in the attenuation of the light energy that is desired to be delivered to the targets.
  • the present invention accounts for the light attenuation of the non-target material present in the fluid by determining the FLEV so that the TELEV may be delivered to the target material.
  • phototherapy systems involve irradiating targets, such as cells or a drug within a cell, with light energy.
  • targets such as cells or a drug within a cell
  • a carrier fluid may be used to deliver the targets for irradiation.
  • the amount of light energy required by a target may be based on the result desired. For example, in CTCL ECP it may be desirable to have a certain percentage of the white blood cells die gradually over a specific period of time after light irradiation treatment (e.g., at least fifty (50) percent of the white blood cells gradually die within six (6) days after irradiation). See PCT Application WO 97/36581 .
  • This light energy value required to produce a desired result e.g., a desired percentage of the targets gradually die over a specified time after exposure to light energy
  • TELEV values may be predetermined and may be available in the memory of a computer system used with the present invention, e . g ., in a look-up table.
  • the FLEV Fluid's Light Energy Value
  • the FLEV is based, in part, on the light attenuation characteristics of the fluid and material therein, and may be determined by the methods and systems of the present invention.
  • Attenuation in the fluid may occur for numerous reasons. For example, attenuation may occur if the fluid being irradiated contains target and/or non-target material that are not entirely transparent. Also, attenuation may occur if the fluid sample being irradiated supports layers of targets and/or non-targets. In addition, the shape and alignment of the individual targets and/or non-targets may influence the quantity of light attenuation.
  • the ALE Factor is 0.1, i.e., only ten (10) percent of the light energy delivered to the surface of the fluid will actually reach (on average) all the targets.
  • 10 Joules (FLEV) of light energy is required to be delivered to the surface of the fluid to ensure that the targets (on average) receive 1 Joule of light energy (the desired result).
  • Buffy coat suspension is partially transparent to the UVA light. Accordingly, this fluid attenuates the irradiance of the light at a given point inside the fluid.
  • the degree of attenuation is a function of absorptivity of the fluid and the light penetration depth from the fluid surface.
  • T 1 10 ⁇ ⁇ a ⁇ c ⁇ D 1
  • a the light absorptivity of the fluid (cm 2 /gr)
  • c the concentration of UVA absorbing component in the fluid (gr/cm 3 ).
  • Equation 2.0 is particularly applicable to partially transparent fluids and, in particular, can be used in photopheresis applications to estimate the average amount of UVA light energy delivered to white blood cells in a well stirred buffy coat suspension.
  • Y is a dimensionless number that represents the geometric shape of the non-target and the stacking factor.
  • the stacking factor is also a dimensionless number that represents the theoretical amount of physical stacking that takes place within the fluid by the non-targets. In ECP applications, for example, the stacking factor may be a number between 1 and 2. Means for obtaining a stacking factor are described in detail supra.
  • Y ⁇ ⁇ R 2 + 2 ⁇ d ⁇ R ⁇ S 2
  • R (cm) is the average radius of the non-target
  • d (cm) is the average thickness of the non-target
  • S is the stacking factor
  • red blood cells have a diameter of about 8 * 10 -4 cm and thickness of about 2 * 10 -4 cm.
  • the first is where all RBC's are evenly distributed in the cube and aligned in such a way that their interference to the UVA irradiation is maximized.
  • the discoid sides of all RBC's are in perpendicular position against the incoming UVA light rays.
  • the second is where all RBC's are evenly distributed in the cube and aligned in such way that their interference to UVA irradiance is minimized.
  • the discoid sides of all RBC's are in parallel position against the incoming UVA light rays.
  • RBC's are preferably randomly distributed in the suspension and the effect of the interference could be somewhere between these two theoretical situations.
  • a one cubic centimeter (or unit volume) of well-mixed buffy coat suspension with UVA light irradiated on one side only is considered.
  • no RBC's were stacked against each other, i.e. no rouleaux formation, because of low hematocrit in buffy coat suspensions.
  • no red blood cells are shielding other red blood cells from UVA light.
  • the first slice will block 5% of the UVA irradiation and the second slice will block additional 5%, and so on.
  • the last layer in the 1/Fa slices will block the last remaining 5% of the UVA light, thereby blocking the light completely. Under this condition about slightly less than half of the fluid, including the target cells within, is irradiated by the UVA light; the remaining portion of the fluid is shielded from the light by the red blood cells.
  • S stacking factor
  • Equations 2.8 and 2.9 represent two opposite extreme cases of RBC light attenuation.
  • Equation 3.1 represents multiples of number of slices, which can block completely the incoming UVA light through one square centimeter area, in one cubic centimeter volume.
  • Ea UVA energy delivered per unit area
  • Ev Eo*A/V
  • Io Incident UVA energy delivered per unit area
  • Joules/cm 2 Io Incident irradiance, Joules/cm 2 -sec.
  • t Irradiation time, seconds.
  • V A*D, Irradiated volume, ml.
  • A Irradiation area
  • cm 2 D Buffy coat film thickness
  • cm C Red blood cell concentration, ⁇ 1.1 * H * 10 8 cells/ml
  • H Hematocrit of the buffy coat suspension
  • % S Stacking factor, dimensionless number between 1 and 2.
  • Equations 2.0 and 2.4 when applied to a fluid containing red blood cells as the dominant attenuating material, predict almost identical ALE factors up to a red blood cell concentration of about 20%, as represented in Figure 10.
  • red blood cell concentrations where the theoretical condition assumed in the stacking equation deviates further from the real situation, the difference between the two equations becomes predictably greater. Indeed, at red blood cell concentrations of over 20% it may be more appropriate to use equation 2.0.
  • equation 3.4 may lose some of its accuracy.
  • Another method for calculating the ALE Factor may utilize the measurements of the uniform thickness of the biological fluid and the red blood cell percentage of the biological fluid.
  • the equations used for this method can be preferably utilized with red blood cell concentrations in the buffy coat suspension of up to twenty (20) percent, and most preferably used with a red blood cell concentration of up to between seven (7) and eight (8) percent
  • the delivery system calculation determines what irradiation time period is needed to deliver the FLEV to the fluid, taking into consideration a variety of factors related to the light source and its present ability to deliver light. This calculation may preferably take into consideration factors such as the shape of the light source, the lamp decay over time, the size of the light beam, and the volume of the fluid being irradiated.
  • the variable L (mW/cm 2 ) accounts for decay of the output of the light source over time and depends upon the properties of the lamp source used, preferably measured at a fixed position from the lamp center line.
  • L may be determined by taking hourly measurements of an exemplary lamp over the lamp's lifetime. As time progresses, the lamp intensity decreases.
  • an equation can be created to match the measurements. Then, the equation can be utilized to determine the value of L by merely knowing how many lamp hours have been used.
  • a database containing the lamp life measurements can be directly accessed.
  • the L value allows one to adjust for lamp life in determining the length of time the light source irradiates the targets to achieve the desired result.
  • an exemplary single lamp irradiance decay equation is determined where a equals 0.78552878, b equals -0.00059106023, and c equals -0.032384473.
  • This equation, as well as the table for L values for the light source utilized, may be stored and accessible for example, in system memory or in a look-up table.
  • the photoactivation chamber is located between two banks of UVA lamps and the buffy coat suspension is recirculated through a serpentine path inside the photoactivation chamber.
  • the blood film thickness in the chamber is the same, about 1.4 mm thick. At this blood film thickness, with hematocrit value at least around few percent, the irradiating UVA light is completely absorbed by the blood film and the total amount of UVA energy delivered to the each ml of circulating buffy coat suspension can be calculated. This value is 255 Joules/ml in the UVAR® system.
  • the irradiance of UVA light reaching the surface of the target cells in the suspension is attenuated by the red blood cells in the light path.
  • the red blood cell is almost completely opaque to the UVA light.
  • the attenuation of the irradiance is inversely proportional to the red blood cell concentration in the light path.
  • the concentration of white blood cells is about one order of magnitude less than that of red blood cells and also the white blood cell is much less opaque to UVA light than red blood cells. Therefore, the amount of attenuation caused by the white blood cells will be insignificant and may be ignored in the derivation of irradiation time equation.
  • UVA energy is delivered through the irradiation chamber and to the surface of the buffy coat suspension film inside the irradiation chamber while the buffy coat film is flowing inside the irradiation chamber.
  • the total amount of UVA energy delivered to the total volume of the buffy coat suspension can be calculated by multiplying the irradiance at blood film surface (through the chamber wall), the irradiation period and the irradiated blood film area.
  • the UVA energy delivered to a unit volume, Ev can be expressed by dividing the total amount of UVA energy delivered divided by the total buffy coat suspension volume.
  • E ⁇ v I ⁇ o ⁇ 1000 ⁇ A ⁇ t ⁇ 60 V
  • Ev UVA energy delivered per unit volume
  • J/ml Io UVA irradiance at blood film surface
  • mW/cm 2 A Area of blood film irradiated inside irradiation chamber
  • 1330 cm 2 t Irradiation period
  • minutes V Total buffy coat suspension volume in the circulation loop, ml.
  • the multiplication factors, 1000 and 60 may be utilized for unit correction from milliwatts to watts and from minutes to seconds.
  • the equation for the average irradiance value, Io, of the UVA light at blood film surface inside the irradiation chamber can be derived as follows.
  • the UVA light reaching the surface of the blood film inside the UVAR® irradiation chamber comes from a light set consisting of nine (9) lamps.
  • the UVA light passes through UVA transparent glass and the acrylic irradiation chamber wall before it reaches the blood film.
  • the UVA output is not uniform along the length of the tubular fluorescence UVA lamp. The output is higher in the middle section of the lamp and lower near the ends of the lamp. Therefore, the average irradiance value of the UVA light reaching the blood film can be obtained by measuring the irradiance at points along the light set and calculating their average value.
  • lamp output decays over time, it is extremely difficult to measure all points simultaneously at a given lamp time. As described below, this problem was resolved by the relationship of this average value to the average single lamp irradiance value at one fixed point that can be measured quickly.
  • Figure 12 shows the average UVA irradiance value of six (6) single lamps measured at mid-point and at a 25 cm distance from the lamp center line as a function of lamp life.
  • the irradiance value decays very rapidly at the beginning and decreases more gradually as the lamp life increases. After around 60 hours of use, the lamp output decays rather slowly and it allows enough time to measure points in the light set and calculate the average irradiance value.
  • the irradiance measurements were made at the 61.5 hour point and the 150 hour point in several light sets. The values were 15.11 and 11.19 mW/cm 2 at 61.5 hours and 150 hours, respectively. The ratios of these average irradiance values in the light box and the average single lamp irradiances at corresponding lamp life were calculated.
  • t min 91.28 ⁇ V ⁇ H T ⁇ k ⁇ L 1
  • t min Irradiation time
  • minutes V Volume of the fluid in the treatment/recirculation loop
  • k 23.9 (a constant based on a ratio of the intensity of one lamp measured at one point in the fluid to the intensity of the entire lamp set in the UVAR® system).
  • the L value at lamp life of 2 hours is 7625 in Figure 11.
  • the L value at lamp life of 3 hours is 7488.
  • the UVAR® instrument in a specific embodiment, uses two lamp banks.
  • the lamp ages of these banks can differ, and theoretically, so can their irradiation time tables.
  • the complete calculation is preferably run twice, once for each lamp bank, and the values may be averaged. This value is the photoactivation time. Once the calculation is run the time remaining is preferably immediately decremented by the amount of time the UV lamps have already been on in the UVAR® system.
  • the present invention contemplates the additional step of delivering the light energy, for that period of time, to the fluid containing targets.
  • the system then may instruct the photoactivation device to deliver the FLEV to the fluid for the determined irradiation period.
  • This may be accomplished via computer or any other known methods.
  • the methods and systems of the present invention contemplate the predetermination of any of the variables such as TELEV, FLEV, thickness ratio, irradiation period, uniform fluid thickness, non-target thickness, and/or hematocrit value in the buffy coat. Any or all of these predetermined variables may be accessible by the user, e.g., available in tabular form, and, in a particular embodiment of the present invention, stored or accessible in computer memory.
  • the irradiation periods were calculated by equations 2.0 and 2.4 to deliver approximately 1.4 Joule/cm 2 of UVA energy to the lymphocytes in the fluids. Since the phosphate buffered saline is transparent to UVA light, the irradiation period was calculated based on the incident irradiance (equation 2.0). The irradiation period for the lymphocytes in the buffy coat suspension was calculated by equations 2.0 and 2.4. The post-irradiation cell viability of both samples was measured to compare the injury to the cells. The cell viability of both samples were around 19% or less seven days after the irradiation while that of the untreated control sample was around 85% or higher. This result shows that the lymphocytes in the phosphate buffered saline and the buffy coat suspension received the same amount of injury and resultant cell death. Indeed, the lymphocytes in both samples received the same amount of UVA energy as calculated by each equation.
  • Equation 2.0 may preferably be used with any partially transparent solutions or suspensions. It requires an accurate transmittance (T) measurement of a known thickness (D) of the fluid, preferably under conditions where the materials in the fluid are homogeneous. Equation 2.4, may be particularly applicable with fluids comprising red blood cells.
  • Figure 1 depicts a extracorporeal photopheresis system 100 as an application of phototherapy according to the present invention as applied to the treatment of leukocytes.
  • the phototherapy system 100 includes a photoactivatable drug, 8-MOP 110, a patient 120, a biological fluid extraction device 130 for extracting blood, a centrifuge device 140 to separate out the buffy coat from the blood, a photoactivation device 150, a fluid ( i . e ., buffy coat) insertion device 160, and a blood insertion device 170.
  • system 100 may contain additional or different devices and can support a variety of phototherapy applications, as mentioned above. See U.S. Patent Nos. 4,921,473 , 4,838,852 , 5,147,289 , 5,150,705 , 5,383,847 , 5,433,738 , and 5,459,322 , each of which :are expressly incorporated by reference herein and relate to various applications to which the systems and apparatus of the present invention can be utilized.
  • FIGS 2A and 2B depict a flow diagram 200 of the blood in the photopheresis system in Figure 1.
  • the first step is to mix the patient's 120 blood with 8-MOP 110 (step 202).
  • the patient 120 is orally administered the 8-MOP 110 and, over the course of a few hours, the drug mixes with the patient's 120 blood.
  • an amount of blood-drug mixture is extracted 130 (step 206) and transferred to a separator, such as a centrifuge device 140 (step 208).
  • the centrifuge device 140 separates the mixture (step 210).
  • a particular centrifuge device uses an optical sensor to determine when to separate (or skim) the fluid. First, the centrifuge skims off the plasma, then the buffy coat, which contains the target material (i . e ., 8-MOP in the leukocytes), and then the red blood cells.
  • the centrifuge device uses an optic sensor located inside the centrifuge chamber that measures deflected light. This optic sensor, by measuring the deflected light in the centrifuge determines when to skim off the separated fluids or material. After separation, the buffy coat and a percentage of plasma are re-combined.
  • the plasma is the medium in which the leukocytes and 8-MOP reside. Even after separation, however, the separated buffy coat and plasma mixture may comprise some red blood cells and platelets, since the separation process may not be able to achieve complete separation. These remaining red blood cells and platelets, contained in the buffy coat, are the non-target attenuators of light. In the present embodiment, the red blood cells are the dominant non-targets since they are the major attenuators of light, when compared to other attenuating material in the target fluid.
  • a second optic sensor determines whether the target fluid contains a desired hematocrit (percentage of red blood cells) (step 212).
  • a desired hematocrit is about one (1) to two (2) percent.
  • This second optic sensor which measures transmittance, determines whether a desired hematocrit is reached (i.e., 1% in the present embodiment). If the hematocrit percentage is not at the desired percentage, then additional blood-drug mixture is processed by the centrifuge (step 210).
  • the centrifuge determines what separated fluid it is processing (step 214). If the centrifuge is processing the non-target fluid, then the centrifuge combines the remaining separated plasma with the separated red blood cells and transfers the mixture to the separated blood insertion device 170 (step 216). Then, the blood insertion device returns the red blood cell/plasma mixture to the patient (step 218) and processing stops.
  • the centrifuge then transfers the target fluid to the photoactivation device (step 220). Step 220 and step 216 may happen concurrently.
  • the photoactivation chamber 150 then irradiates the fluid for a period of time (step 222).
  • Computer 300 controls the photoactivation chamber 150 as illustrated in Figure 3 and described in the corresponding discussion.
  • the target fluid, now treated, is then transferred to a fluid insertion device 160 (step 224). Then, the target insertion device returns the red blood cell/plasma mixture to the patient (step 226) and processing stops.
  • FIG. 3 is a diagram of a computer 300 for controlling the photoactivation device 150 according to the implementation of the present invention.
  • the computer 300 includes a memory 310, a central processing unit (CPU) 320, a photoactivation interface 330, an operator interface 340, an input device 350, and a video display 360.
  • CPU central processing unit
  • the memory 310 further includes an operating system 312, a photoactivation program 314, and look-up table 315.
  • the look-up table 315 may comprise a storage location in the memory 310 and may contain tables that correspond to data needed by the photoactivation program 314. The individual tables and the corresponding data are described in further detail in the descriptions that correspond to Figures 4 through 9.
  • the photoactivation program 312 acquires the FLEV.
  • the FLEV could be obtained by accessing the look-up table 315, via the input device 350, or by calculation as further described in the descriptions that correspond to Figures 4 through 9.
  • FIG. 4 depicts a flowchart 400 of the steps performed by the photoactivation program 314 when requested to determine and then deliver an amount of light energy to a fluid containing targets whereby the targets in the fluid will receive an effective amount of light energy.
  • the first step performed by the photoactivation program 314 is to obtain the TELEV (step 402).
  • the desired result is previously defined and is based on the phototherapy application. For instance, when photopheresis is used to treat CTCL, the TELEV applied to the leukocytes preferably causes at least fifty (50) percent of the leukocytes to gradually die within six (6) days after exposure to the light energy.
  • the TELEV may be obtained by accessing, for example, a look-up table 315 that contains TELEV data.
  • the photoactivation program 314 may obtain the TELEV via the input device 350.
  • Figure 5 illustrates how the TELEV may be clinically identified once the desired result is known.
  • the next step is to obtain the average light energy factor for the fluid (step 404).
  • the ALE factor is the percent of incident light energy that will be delivered to an average unit area of fluid.
  • the ALE factor may be obtained by accessing the portion of the look-up table 315 that pertains to ALE factor data. In an alternative embodiment of the present invention, the ALE factor may be obtained via the input device 350.
  • the ALE factor may be obtained for any target in a biological fluid from knowing the average light energy value (Joules/cm 2 ) at the unit surface area of the targets in the fluid and knowing the light energy value (Joules/cm 2 ) at the incident surface of the biological fluid.
  • the description that accompanies Figure 6 illustrates such a procedure for obtaining the ALE factor.
  • the ALE factor may be obtained from knowing the fluid's thickness ratio and the light transmittance value of a known fluid thickness.
  • the thickness ratio is the ratio of the uniform thickness of the fluid and the average thickness of the non-target in the fluid.
  • the non-target is material in the fluid that attenuates light energy. The description that accompanies Figure 7 illustrates such a procedure for obtaining the ALE factor.
  • the ALE factor when fluid comprises red blood cells as non-targets that attenuate light energy, the ALE factor may be obtained from knowing the thickness ratio and knowing the percentage of hematocrit or red blood cells in the fluid.
  • the description that accompanies Figure 8 illustrates such a procedure for obtaining the ALE factor.
  • the ALE factor when fluid comprises red blood cells as non-targets that attenuate light energy, the ALE factor may be obtained from knowing the uniform thickness of the fluid and knowing the percentage of hematocrit or red blood cells in the fluid.
  • the description that accompanies Figure 9 illustrates such a procedure for obtaining the ALE factor.
  • the next step is to obtain the FLEV or the amount of light energy needed to be delivered to the fluid so that the targets in the fluid will receive the TELEV (step 406).
  • the FLEV can be calculated by knowing the TELEV and the ALE factor and using equation 1.0, as described previously.
  • the irradiation time period is the amount of time needed for the lamp or light energy source to deliver the FLEV to the fluid.
  • the irradiation time period is obtained by accessing the portion of the look-up table 315 that pertains to irradiation time period data.
  • the irradiation time period can be calculated. Factors that might be considered in irradiation time period calculation are lamp decay or power, the shape of the lamp, or the volume of fluid to be irradiated.
  • the irradiation time period can be calculated knowing the fluid's volume, the percent of red-blood cells in the fluid, and the decay life of the light source using, for example, an equation such as equation 1.5, as described previously.
  • the photoactivation device 150 may then instruct the photoactivation device 150 to engage the light energy lamp for the irradiation time period.
  • FIG. 5 depicts a flowchart 500 of the steps performed when clinically obtaining the TELEV.
  • the first step in clinically obtaining the TELEV is to obtain the desired result of the phototherapy (step 502).
  • the next step is to place sample targets in a non-attenuating fluid, which is often a biological or chemical fluid (step 504).
  • a non-attenuating fluid which is often a biological or chemical fluid.
  • targets such as saline, and filtered plasma.
  • samples of the fluid can be used for the clinical tests, provided any or most of the non-attenuation materials are filtered out.
  • samples of the fluid containing the targets are irradiated with varying amounts of light energy (step 506).
  • a TELEV is identified that corresponds to the sample that produced the desired the result (step 508).
  • any TELEV is specific to the particular application of the methods and systems of the present invention.
  • Figure 6 depicts a flowchart 600 of the steps performed by the photoactivation program 314 when obtaining the ALE factor.
  • This procedure for obtaining the ALE factor may be used for any fluid containing targets.
  • the first step to obtain the ALE factor is to obtain the average light energy value at the unit surface area of the targets in the fluid (step 602).
  • the average light energy value at the unit surface area can be obtained by accessing the portion of the look-up table 315 that pertains to average light energy value at the unit surface area data.
  • the photoactivation program 314 may obtain the average light energy value at the unit surface area via the input device 350.
  • the next step is to obtain the light energy value at the incident surface of the biological fluid (step 604).
  • the light energy value at the incident surface can be obtained by accessing the portion of the look-up table 315 that pertains to light energy value at the incident surface data.
  • the photoactivation program 314 may obtain the light energy value at the incident surface via the input device 350.
  • the ALE factor may then be calculated using equation 1.0 (step 606).
  • Figure 7 depicts a flowchart 700 of the steps performed by the photoactivation program 314 when obtaining the ALE factor.
  • This procedure for obtaining the ALE factor may be used for any biological fluid containing targets. However, the accuracy of this equation is maximized when a homogeneous mixture of targets and non-targets in the fluid is provided.
  • a homogeneous biological fluid mixture may be obtained by stirring the biological fluid containing the targets and non-targets.
  • the thickness ratio is the ratio of the uniform thickness of the fluid and the average thickness of the non-target in the fluid.
  • the thickness ratio, the uniform fluid thickness, and the non-target's thickness can be obtained by obtaining these values by, for example, accessing a look-up table 315 that contains data relating to these parameters.
  • the photoactivation program 314 may obtain the thickness ratio, the uniform fluid thickness, and the non-target thickness via the input device 350. Once the uniform fluid thickness and the non-target thickness data are obtained, the thickness ratio can be calculated by dividing the uniform fluid thickness by the non-target thickness.
  • a light transmittance value of a known fluid thickness (step 704).
  • the irradiation period can be obtained by accessing the portion of a look-up table 315 that pertains to light transmittance value of a known fluid thickness data.
  • the photoactivation program 314 may obtain a light transmittance value of a known fluid thickness.
  • the ALE factor may then be calculated using equation 1.1 (step 706).
  • Figure 8 depicts a flowchart 800 of the steps performed by the photoactivation program 314 when obtaining the ALE factor.
  • This procedure for obtaining the ALE factor may be used for biological fluid that comprises red blood cells as non-targets that attenuate light energy. The accuracy of this equation may depend on how well the fluid is stirred.
  • the first step to obtain the ALE factor is to obtain the thickness ratio (step 802).
  • the thickness ratio is the ratio of the uniform thickness of the fluid and the average thickness of the non-target in the fluid.
  • the non-target is the material in the fluid that attenuates light energy.
  • the thickness ratio, the uniform fluid thickness, and the non-target's thickness can be obtained by accessing the portion of the look-up table 315 that pertains to thickness ratio, the uniform fluid thickness, and the non-target thickness data, respectively.
  • the photoactivation program 314 may obtain the thickness ratio, the uniform fluid thickness, and the non-target's thickness via the input device 350. Once obtaining the uniform fluid thickness and the non-target thickness data, the thickness ratio can be calculated by dividing the uniform fluid thickness by the non-target thickness.
  • the next step is to obtain percentage of red blood cells or hematocrit per unit of biological fluid (step 804).
  • the red-blood cell percentage can be obtained by reading, for example, the optical or electromagnetic profile of the fluid by known means or by accessing the portion of the look-up table 315 that pertains to red-blood cell percentage data.
  • the photoactivation program 314 may obtain the red-blood cell percentage via the input device 350.
  • the ALE factor may then be calculated using equation 1.2 (step 806).
  • Figure 9 depicts a flowchart 900 of the steps performed by the photoactivation program 314 when obtaining the ALE factor.
  • This procedure for obtaining the ALE factor may be used for biological fluid that comprises red blood cells as non-targets that attenuate light energy and have a stacking factor of between 1 and 2. The accuracy of the results of this equation may depend on how well the fluid is stirred.
  • the first step to obtain the ALE factor is to obtain the uniform fluid thickness (step 802).
  • the uniform fluid thickness can be obtained by accessing the portion of the look-up table 315 that pertains to uniform fluid thickness data.
  • the photoactivation program 314 may obtain the uniform fluid thickness via the input device 350.
  • the next step is to obtain the percentage of red blood cells or hematocrit per unit of biological fluid (step 904).
  • the red blood cell percentage can be obtained by reading, for example, the optical or electromagnetic profile of the fluid by known means or by accessing the portion of the look-up table 315 that pertains to red blood cell percentage data.
  • the photoactivation program 314 may obtain the red blood cell percentage via the input device 350.
  • the ALE factor may then be calculated using equation 1.3 (step 906).
  • Figure 10 depicts a graph of ALE factors calculated for a fluid comprising red blood cells as non-targets for three different fluid thicknesses (1 mm, 2 mm, and 3 mm). These ALE factors were calculated using equations 1.1 (Analytical Model) and 1.3 (Stacking Model). The ratio of the average light energy delivered to the targets in the fluid and the light energy delivered to the incident point is plotted as a function of percent hematocrit at different fluid thickness.

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3354300A1 (fr) * 2017-01-30 2018-08-01 Fenwal, Inc. Systèmes et procédés permettant de recueillir des cellules mononucléaires ayant un taux d'hématocrite approprié pour une photophérèse extracorporelle

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6969367B2 (en) * 2000-02-02 2005-11-29 Xepmed, Inc. Extracorporeal pathogen reduction system
US7470245B2 (en) * 2000-02-02 2008-12-30 Xepmed, Inc. Extracorporeal pathogen reduction system
CA2475021A1 (fr) * 2001-01-31 2002-08-08 Dror Mevorach Induction de tolerance par des cellules apoptotiques et/ou necrotiques
US20050202098A1 (en) * 2001-01-31 2005-09-15 Tolaren Disease therapy using dying or dead cells
US20030157073A1 (en) * 2001-11-29 2003-08-21 Peritt David L. Methods for pretreating a subject with apoptotic cells
US7186230B2 (en) * 2002-03-04 2007-03-06 Therakos, Inc Method and apparatus for the continuous separation of biological fluids into components
US7479123B2 (en) * 2002-03-04 2009-01-20 Therakos, Inc. Method for collecting a desired blood component and performing a photopheresis treatment
US20040127840A1 (en) 2002-03-04 2004-07-01 Steve Gara Blood separation apparatus and method of using the same
US7211037B2 (en) * 2002-03-04 2007-05-01 Therakos, Inc. Apparatus for the continuous separation of biological fluids into components and method of using same
US20050049539A1 (en) * 2003-09-03 2005-03-03 O'hara Gerald P. Control system for driving fluids through an extracorporeal blood circuit
US20050101997A1 (en) * 2003-11-12 2005-05-12 Reddy Vivek Y. Arrangements and methods for determining or treating cardiac abnormalities and inconsistencies
AU2004237844B2 (en) 2003-12-23 2011-01-27 Therakos, Inc. Extracorporeal photopheresis in combination with anti-TNF treatment
US8296071B2 (en) * 2004-03-15 2012-10-23 Terumo Bct Biotechnologies, Llc Methods for uniformly treating biological samples with electromagnetic radiation
US7476209B2 (en) * 2004-12-21 2009-01-13 Therakos, Inc. Method and apparatus for collecting a blood component and performing a photopheresis treatment
DE102005022608B3 (de) * 2005-05-11 2007-01-11 Karl Storz Gmbh & Co. Kg Lichtsystem zur photodynamischen Diagnose und/oder Therapie
EP1928549B1 (fr) * 2005-09-28 2014-06-11 Candela Corporation Appareil pour le traitement de cellulite
US9169461B2 (en) * 2005-11-02 2015-10-27 Therakos, Inc. Use of apoptotic cells ex vivo to generate regulatory T cells
CN101484586A (zh) 2006-05-02 2009-07-15 特拉科斯有限公司 检测移植物抗宿主疾病易感性或移植相关死亡率的方法和试剂
WO2011040535A1 (fr) * 2009-09-30 2011-04-07 東レ株式会社 Composition vaccinale contre le virus de l'hépatite c
US9399093B2 (en) * 2012-01-27 2016-07-26 Fenwal, Inc. Systems and methods for performing online extracorporeal photopheresis
WO2014123521A1 (fr) 2013-02-06 2014-08-14 Fenwal, Inc. Procédé pour administrer une dose de lumière désirée à des cellules dans un milieu atténuant de la lumière
US10172995B2 (en) 2013-02-06 2019-01-08 Fenwal, Inc. System and method for determining irradiation exposure time with irradiation sensors during extracorporeal photopheresis
US10213544B2 (en) 2013-06-13 2019-02-26 Fenwal, Inc. Methods for treating a suspension of mononuclear cells to facilitate extracorporeal photopheresis
GB2525432A (en) * 2014-04-24 2015-10-28 Univ Oslo Hf Modification of extracorporeal photopheresis technology with porphyrin precursors
US20160114095A1 (en) * 2014-10-27 2016-04-28 Fenwal, Inc. Methods and systems for collecting mononuclear cells
JP6632359B2 (ja) * 2015-01-05 2020-01-22 フェンウォール、インコーポレイテッド 体外フォトフェレーシスにおいて照射受光部を用いて最小ヘマトクリットを検出するためのシステムと方法
EP3552637B1 (fr) 2015-02-06 2022-09-28 Fenwal, Inc. Système permettant de déterminer la durée d'exposition d'irradiation par des capteurs de lumière lors de photophérèse extracorporelle
ES2792991T3 (es) 2015-06-19 2020-11-12 Mallinckrodt Hospital Products Ip Ltd Dispositivos, métodos y sistemas para cebar, separar y recoger componentes sanguíneos
US10434240B2 (en) 2015-08-17 2019-10-08 Fenwal, Inc. Methods and systems for processing and washing a photopheresis mononuclear cell product
GB201604246D0 (en) * 2016-03-11 2016-04-27 Univ Hull Radioactivity detection
WO2020174547A1 (fr) * 2019-02-25 2020-09-03 大塚電子株式会社 Dispositif de thérapie photodynamique

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236999A (en) * 1962-10-01 1966-02-22 North American Aviation Inc Computer having floating point division
US4464336A (en) * 1980-05-15 1984-08-07 Ushio Denki Kabushikikaisha Method of sterilization
DE3739966A1 (de) * 1987-11-25 1989-06-08 Katadyn Produkte Ag Vorrichtung zur desinfektion von wasser durch uv-bestrahlung
WO1990006899A1 (fr) * 1988-12-13 1990-06-28 Dr. K. Hönle Gmbh Dispositif de sterilisation de liquides aux rayons ultra-violets
US5030200A (en) * 1987-06-25 1991-07-09 Baylor Research Foundation Method for eradicating infectious biological contaminants in body tissues
WO1997015332A1 (fr) * 1995-10-26 1997-05-01 Purepulse Technologies, Inc. Desactivation amelioree d'organismes utilisant une lumiere polychromatique pulsee a haute intensite
US5768853A (en) * 1996-02-15 1998-06-23 Purepulse Technologies, Inc. Deactivation of microorganisms

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4196281A (en) 1976-10-20 1980-04-01 Regents Of The University Of California Psoralens
US4260630A (en) * 1977-08-29 1981-04-07 Agence Nationale De Valorisation De La Recherche (Anvar) Skin diseases
IT1088554B (it) 1977-11-17 1985-06-10 F I D I A Spa Procedimento sellettivo per la preparazione di derivati della 7-indrossi cumarina
US4428744A (en) 1979-12-11 1984-01-31 Frederic A. Bourke, Jr. Method and system for externally treating the blood
US4398906A (en) 1979-12-11 1983-08-16 Frederic A. Bourke, Jr. Method for externally treating the blood
US4321919A (en) 1979-12-11 1982-03-30 Leukocyte Research, Inc. Method and system for externally treating human blood
US4464166A (en) 1981-06-12 1984-08-07 Frederic A. Bourke, Jr. Method for externally treating the blood
US4612007A (en) 1981-06-16 1986-09-16 Edelson Richard Leslie Method and system for externally treating the blood
FR2521999B1 (fr) 1982-02-25 1984-05-25 Inst Nat Sante Rech Med Pyrido (3',4' : 4,5) furo (3,2-g) coumarines ou pyrido (3,4-h) psoralenes, obtention, applications en cosmetologie et a titre de medicaments, et compositions cosmetiques et pharmaceutiques les contenant
FR2521998B1 (fr) 1982-02-25 1985-10-25 Inst Nat Sante Rech Med Pyrido (3,4-c) psoralenes, obtention, applications en cosmetologie et a titre de medicaments et compositions cosmetiques et pharmaceutiques les contenant
US4613322A (en) 1982-12-08 1986-09-23 Edelson Richard Leslie Method and system for externally treating the blood
US4684521A (en) 1982-12-08 1987-08-04 Frederic A. Bourke, Jr. Method and system for externally treating the blood
US4683889A (en) 1983-03-29 1987-08-04 Frederic A. Bourke, Jr. Method and system for externally treating the blood
US4748120A (en) 1983-05-02 1988-05-31 Diamond Scientific Co. Photochemical decontamination treatment of whole blood or blood components
US4727027A (en) 1983-05-02 1988-02-23 Diamond Scientific Co. Photochemical decontamination treatment of whole blood or blood components
US5176921A (en) 1983-05-02 1993-01-05 Diamond Scientific Co. Method of blood component decontamination by glucose addition
CA1253115A (fr) * 1983-09-29 1989-04-25 Extracorporeal Medical Specialties, Inc. Appareil et methodes pour traiter des cellules a l'aide de radiations
US4693981A (en) 1983-12-20 1987-09-15 Advanced Genetics Research Institute Preparation of inactivated viral vaccines
US4573961A (en) 1984-10-29 1986-03-04 Extracorporeal Medical Specialties, Inc. Electronic control methods for puvapheresis apparatus
US4708715A (en) 1984-10-29 1987-11-24 Mcneilab, Inc. Light array assembly for photoactivation patient treatment system
US4596547A (en) 1984-10-29 1986-06-24 Mcneilab, Inc. Valve apparatus for photoactivation patient treatment system
US4687464A (en) 1984-10-29 1987-08-18 Mcneilab, Inc. Zero insertion force socket for photoactivation patient treatment system
US4705498A (en) 1984-10-29 1987-11-10 Mcneilab, Inc. Disposable temperature probe for photoactivation patient treatment system
US4623328A (en) 1984-10-29 1986-11-18 Mcneilab, Inc. Pump monitor for photoactivation patient treatment system
US4737140A (en) 1984-10-29 1988-04-12 Mcneilab, Inc. Irradiation chamber for photoactivation patient treatment system
US4568328A (en) 1984-10-29 1986-02-04 Extracorporeal Medical Specialties, Inc. Automated photophoresis blood portion control methods and apparatus
US4692138A (en) 1984-10-29 1987-09-08 Mcneilab, Inc. Pump block for interfacing irradiation chamber to photoactivation patient treatment system
US4573962A (en) 1984-10-29 1986-03-04 Extracorporeal Medical Specialties, Inc. Cassette drawer assembly for photoactivation patient treatment system
US4681568A (en) 1984-10-29 1987-07-21 Mcneilab, Inc. Valve apparatus for photoactivation patient treatment system
US4573960A (en) 1984-10-29 1986-03-04 Extracorporeal Medical Specialties, Inc. Three phase irradiation treatment process
US4578056A (en) 1984-10-29 1986-03-25 Extracorporeal Medical Specialties, Inc. Patient photopheresis treatment apparatus and method
US4643710A (en) 1984-10-29 1987-02-17 Mcneilab, Inc. Valve apparatus for photoactivation patient treatment system
US4608255A (en) * 1985-01-31 1986-08-26 American National Red Cross Biocompatible method for in situ production of functional platelets and product produced thereby lacking immunogenicity
USD299531S (en) 1986-02-27 1989-01-24 Mcneilab, Inc. Patient photopheresis treatment unit
USD298567S (en) 1986-02-27 1988-11-15 Mcneilab, Inc. Flexible patient fluid container
USD299953S (en) 1986-02-27 1989-02-21 Mcneilab, Inc. Control panel for a patient photophoresis treatment unit
US4897789A (en) 1986-02-27 1990-01-30 Mcneilab, Inc. Electronic device for authenticating and verifying disposable elements
USD298279S (en) 1986-02-27 1988-10-25 Mcneilab, Inc. Disposable patient fluid irradiation chamber
US4866282A (en) 1986-08-26 1989-09-12 Baxter International Inc. Irradiation of blood products
US4952812A (en) 1986-08-26 1990-08-28 Baxter International Inc. Irradiation of blood products
US4726949A (en) 1986-08-26 1988-02-23 Baxter Travenol Laboratories, Inc. Irradiation of blood products
US4838852A (en) 1987-03-27 1989-06-13 Therakos, Inc. Active specific immune suppression
US4960408A (en) 1989-01-10 1990-10-02 Klainer Albert S Treatment methods and vaccines for stimulating an immunological response against retroviruses
US5216176A (en) 1989-01-23 1993-06-01 Lehigh University 7-alkoxycoumarins, dihydropsoralens, and benzodipyranones as photo-activated therapeutic agents and inhibitors of epidermal growth factor
US5356929A (en) 1989-01-23 1994-10-18 Lehigh University Reduced and quaternized psoralens as photo-activated therapeutics
US4921473A (en) 1989-02-02 1990-05-01 Therakos, Inc. Multicomponent fluid separation and irradiation system
US4999375A (en) 1989-04-11 1991-03-12 Hoffmann-La Roche Inc. Psoralen reagent compositions for extracorporeal treatment of blood
CA2089005C (fr) 1991-06-21 1999-01-19 John Chapman Methode d'inactivation des agents pathogenes dans les liquides organiques
WO1993014791A2 (fr) 1992-01-27 1993-08-05 Cryopharm Corporation Procede d'inactivation des contaminants viraux et bacteriens du sang
CN1022167C (zh) * 1992-02-21 1993-09-22 第四军医大学西京医院临床输血研究中心 光量子血液治疗仪
US5618662A (en) * 1992-03-02 1997-04-08 Cerus Corporation Intravenous administration of psoralen
US5459030A (en) 1992-03-02 1995-10-17 Steritech, Inc. Synthetic media compositions for inactivating bacteria and viruses in blood preparations with 8-methoxypsoralen
US5288605A (en) 1992-03-02 1994-02-22 Steritech, Inc. Methods for inactivating bacteria in blood preparations with 8-methoxypsoralen
ATE192898T1 (de) 1992-08-07 2000-06-15 Cerus Corp Verfahren zur inaktivierung von bakterien in blutpräparaten mit hilfe von methoxypsoralen
US5820872A (en) 1992-11-18 1998-10-13 Yale University Methods and compositions for improving the effectiveness of X-irradiation therapy for the treatment of an internal solid tumor
US5651993A (en) 1992-11-18 1997-07-29 Yale University Specific immune system modulation
CN1080547A (zh) * 1993-05-22 1994-01-12 第四军医大学西京医院临床输血研究中心 光量子血液治疗仪
US5459322A (en) * 1993-12-14 1995-10-17 Therakos, Inc. Ultraviolet light chamber
US5522868A (en) * 1994-08-23 1996-06-04 Sisters Of Providence In Oregon Method and apparatus for determination of psoralen concentrations in biological tissues
US5925034A (en) * 1994-08-23 1999-07-20 Sisters Of Providence In Oregon Method and apparatus for determination of psoralen concentrations in biological tissues
US5845255A (en) * 1994-10-28 1998-12-01 Advanced Health Med-E-Systems Corporation Prescription management system
JP2000510101A (ja) 1996-03-29 2000-08-08 セラコス・インコーポレーテツド 白血球のフォトフェレーシス処置
AU717624B2 (en) 1996-03-29 2000-03-30 Therakos, Inc. Photopheresis treatment of chronic HCV infections
US5922278A (en) * 1996-11-19 1999-07-13 Baxter International Inc. Method and apparatus for inactivating contaminants in biological fluid
ATE350083T1 (de) 1996-11-22 2007-01-15 Therakos Inc Apparat mit rührvorrichtung zur bestrahlung eines blutproduktes

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236999A (en) * 1962-10-01 1966-02-22 North American Aviation Inc Computer having floating point division
US4464336A (en) * 1980-05-15 1984-08-07 Ushio Denki Kabushikikaisha Method of sterilization
US5030200A (en) * 1987-06-25 1991-07-09 Baylor Research Foundation Method for eradicating infectious biological contaminants in body tissues
DE3739966A1 (de) * 1987-11-25 1989-06-08 Katadyn Produkte Ag Vorrichtung zur desinfektion von wasser durch uv-bestrahlung
WO1990006899A1 (fr) * 1988-12-13 1990-06-28 Dr. K. Hönle Gmbh Dispositif de sterilisation de liquides aux rayons ultra-violets
WO1997015332A1 (fr) * 1995-10-26 1997-05-01 Purepulse Technologies, Inc. Desactivation amelioree d'organismes utilisant une lumiere polychromatique pulsee a haute intensite
US5768853A (en) * 1996-02-15 1998-06-23 Purepulse Technologies, Inc. Deactivation of microorganisms

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3354300A1 (fr) * 2017-01-30 2018-08-01 Fenwal, Inc. Systèmes et procédés permettant de recueillir des cellules mononucléaires ayant un taux d'hématocrite approprié pour une photophérèse extracorporelle
US10556053B2 (en) 2017-01-30 2020-02-11 Fenwal, Inc. System for collecting mononuclear cells having a suitable hematocrit for extracorporeal photopheresis

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TR200001913A2 (tr) 2001-02-21
DK1066842T3 (da) 2006-10-23
CN100354623C (zh) 2007-12-12
IL137133A0 (en) 2001-07-24
US6219584B1 (en) 2001-04-17
IL137133A (en) 2005-07-25
EP1754497B1 (fr) 2009-06-03
PT1754497E (pt) 2009-07-27
DE60028872T2 (de) 2006-12-28
EP1066842A2 (fr) 2001-01-10
JP2001054579A (ja) 2001-02-27
SG89337A1 (en) 2002-06-18
HU0002591D0 (en) 2000-08-28
ES2327951T3 (es) 2009-11-05
DE60028872D1 (de) 2006-08-03
NO20003522L (no) 2001-01-10
CA2313577A1 (fr) 2001-01-09
CA2313577C (fr) 2019-02-12
HK1033101A1 (en) 2001-08-17
HUP0002591A2 (hu) 2001-06-28
ATE330648T1 (de) 2006-07-15
CZ20002547A3 (cs) 2001-02-14
EP1066842B1 (fr) 2006-06-21
NO20003522D0 (no) 2000-07-07
CN1296171A (zh) 2001-05-23
PT1066842E (pt) 2006-09-29
DE60042349D1 (de) 2009-07-16
JP5008788B2 (ja) 2012-08-22
ATE432725T1 (de) 2009-06-15
EP1066842A3 (fr) 2002-07-17
ES2265869T3 (es) 2007-03-01
CZ302538B6 (cs) 2011-07-07

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